ISRCTN11058680进行中（未招募）未知
The randomised thoracoscopic talc poudrage and indwelling pleural catheters versus thoracoscopic talc poudrage only in malignant pleural effusion trial
orth Bristol NHS Trust0 个研究点目标入组 124 人开始时间: 2021年8月23日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 124
研究概览
简要总结
2023 Protocol article in https://pubmed.ncbi.nlm.nih.gov/37253535/ protocol (added 31/05/2023)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Symptomatic pleural effusion and any of the following:
- •1.1. Thoracoscopically confirmed evidence of malignant pleural disease (visible cancer at thoracoscopy) which requires talc poudrage as part of routine clinical care
- •1.2. An established diagnosis of malignant pleural effusion (via biopsy or cytology) which requires drainage and pleurodesis as per standard care, where the patient/operator decide on a thoracoscopic treatment
- •1.3. Symptomatic effusion requiring drainage and pleurodesis in the context of established metastatic disease
- •2. Able to consent to trial inclusion
排除标准
- •1. Technically unable to undergo thoracoscopy and talc poudrage (e.g. gross respiratory failure, uncorrectable clotting, unable to tolerate position, significant suspicion of underlying trapped lung or poor performance status)
- •2. Visual impairment (precluding use of symptom measurement instruments)
- •3. Previous talc pleurodesis within the last 3 months on ipsilateral side
- •4. No means of phone contact
- •5. Age <18 years
- •6. Females who are pregnant or lactating
- •7. Unable to consent to trial inclusion
研究者
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